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Elfride De Baere

Showing results (1-10 of 210) with videos related to

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Human Mutation|July 22, 2014
Deciphering the cis-regulatory landscape of SOX9 implicated in craniofacial development and isolated Pierre Robin sequenceElfride De Baere
Investigative Ophthalmology & Visual Science|September 10, 2014
Heterozygous coding ZNF469 variants enriched in New Zealand patients with isolated keratoconusElfride De Baere
Hormone Research in Paediatrics|January 18, 2012
FOXL2 impairment in human diseaseHannah Verdin, Elfride De Baere
The Journal of Clinical Endocrinology and Metabolism|July 2, 2025
Approach to the patient with a difference of sexual developmentHannes Syryn, Elfride De Baere, Martine Cools
Human Mutation|August 30, 2008
FOXL2 mutations and genomic rearrangements in BPESDiane Beysen, Anne De Paepe, Elfride De Baere
Folia Histochemica Et Cytobiologica|January 14, 2010
The transcription factor FOXL2 in ovarian function and dysfunctionElfride De Baere, Marc Fellous, Reiner A Veitia
European Journal of Human Genetics : EJHG|October 14, 2010
Clinical utility gene card for: Axenfeld-Rieger syndromeNicole Weisschuh, Elfride De Baere, Bernd Wissinger, et al.
Best Practice & Research. Clinical Endocrinology & Metabolism|April 22, 2019
Update on the genetics of differences of sex development (DSD)Dorien Baetens, Hannah Verdin, Elfride De Baere, et al.
European Journal of Human Genetics : EJHG|July 5, 2018
Incidental or secondary findings: an integrative and patient-inclusive approach to the current debateMarlies Saelaert, Heidi Mertes, Elfride De Baere, et al.
Genetics|December 12, 2003
Compositional biases and polyalanine runs in humansJulie Cocquet, Elfride De Baere, Sandrine Caburet, et al.
Pageof 21

Showing results (1-10 of 210) with videos related to

Sort By:
Pageof 21
Human Mutation|July 22, 2014
Deciphering the cis-regulatory landscape of SOX9 implicated in craniofacial development and isolated Pierre Robin sequenceElfride De Baere
Investigative Ophthalmology & Visual Science|September 10, 2014
Heterozygous coding ZNF469 variants enriched in New Zealand patients with isolated keratoconusElfride De Baere
Hormone Research in Paediatrics|January 18, 2012
FOXL2 impairment in human diseaseHannah Verdin, Elfride De Baere
The Journal of Clinical Endocrinology and Metabolism|July 2, 2025
Approach to the patient with a difference of sexual developmentHannes Syryn, Elfride De Baere, Martine Cools
Human Mutation|August 30, 2008
FOXL2 mutations and genomic rearrangements in BPESDiane Beysen, Anne De Paepe, Elfride De Baere
Folia Histochemica Et Cytobiologica|January 14, 2010
The transcription factor FOXL2 in ovarian function and dysfunctionElfride De Baere, Marc Fellous, Reiner A Veitia
European Journal of Human Genetics : EJHG|October 14, 2010
Clinical utility gene card for: Axenfeld-Rieger syndromeNicole Weisschuh, Elfride De Baere, Bernd Wissinger, et al.
Best Practice & Research. Clinical Endocrinology & Metabolism|April 22, 2019
Update on the genetics of differences of sex development (DSD)Dorien Baetens, Hannah Verdin, Elfride De Baere, et al.
European Journal of Human Genetics : EJHG|July 5, 2018
Incidental or secondary findings: an integrative and patient-inclusive approach to the current debateMarlies Saelaert, Heidi Mertes, Elfride De Baere, et al.
Genetics|December 12, 2003
Compositional biases and polyalanine runs in humansJulie Cocquet, Elfride De Baere, Sandrine Caburet, et al.
Pageof 21